Job summary
Job post source
This job is directly from Worldwide Clinical Trials
Job overview
The Senior Medical Writer role at Worldwide Clinical Trials involves leading medical writing teams to prepare regulatory and clinical study documents, impacting the quality and compliance of clinical trial documentation globally.
Responsibilities and impact
The role requires preparing and leading the creation of Phase I-IV study documents, collaborating with other departments on regulatory submissions, managing document templates, and serving as a publishing contact for clinical trial reports.
Compensation and benefits
The salary range is $80,735 to $160,265, with compensation varying by skills, experience, and location; specific benefits are not detailed but the company emphasizes a supportive and inclusive work environment.
Experience and skills
Candidates need a life science degree or equivalent experience, at least 4 years as a Medical Writer or similar role, excellent English skills, regulatory knowledge (ICH E3, E6, E9), strong project management, and Microsoft Office proficiency; availability for domestic and international travel is required.
Career development
The company offers ongoing training and career development opportunities within a dynamic global medical writing team.
Work environment and culture
Worldwide Clinical Trials promotes a diverse, inclusive, and collaborative culture with accessible leadership and supportive teams, encouraging employees to thrive and be their best.
Company information
Worldwide Clinical Trials is a global midsize CRO with over 3,500 employees focused on innovative clinical research to improve patient lives worldwide.
Team overview
The medical writing team is global, dynamic, and well-supported, working closely with subject matter experts and regulatory strategists across the company.
Job location and travel
The position is remote, supporting UK/US candidates, with domestic and international travel required.
Unique job features
The role offers unique opportunities to work on a wide range of clinical documents across multiple regulatory regions and therapeutic areas, with leadership responsibilities in medical writing.
Company overview
Worldwide Clinical Trials is a global contract research organization (CRO) that provides phase I-IV clinical trial services to the pharmaceutical and biotechnology industries. They specialize in therapeutic areas such as neuroscience, cardiovascular, metabolic, and rare diseases. Founded in 1986, the company has grown to operate in more than 60 countries, leveraging their scientific expertise and innovative technologies to deliver high-quality data and support drug development. Their revenue is primarily generated through service contracts with pharmaceutical companies, offering comprehensive clinical trial management, data analysis, and regulatory support.
How to land this job
Tailor your resume to highlight medical writing expertise, especially in preparing Phase I-IV clinical trial documents, regulatory submissions, and adherence to ICH guidelines such as E3, E6, and E9.
Emphasize your experience working cross-functionally with clinical, regulatory, and publishing teams, showcasing your ability to manage multiple projects and meet tight deadlines independently.
Apply through Worldwide Clinical Trials' official corporate careers page and also submit your application via LinkedIn and other reputable job boards to maximize exposure.
Connect with current Worldwide Clinical Trials medical writing team members or regulatory affairs professionals on LinkedIn; start conversations by referencing recent company innovations or asking about their experiences with global regulatory submissions.
Optimize your resume for ATS by incorporating keywords like 'clinical trial reports,' 'protocol amendments,' 'ICH E3/E6/E9,' 'regulatory submissions,' and 'medical writing leadership' to ensure your resume passes automated screening filters.
Use Jennie Johnson's Power Apply feature to automate tailored resume customization, multi-channel applications, and LinkedIn networking, freeing you to focus on interview preparation and skill enhancement.
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